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Identification of a Biomarker in Cerebrospinal Fluid for Neuronopathic Forms of Gaucher Disease
Gaucher disease, a recessive inherited metabolic disorder caused by defects in the gene encoding glucosylceramidase (GlcCerase), can be divided into three subtypes according to the appearance of symptoms associated with central nervous system involvement. We now identify a protein, glycoprotein non-...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4361053/ https://ncbi.nlm.nih.gov/pubmed/25775479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0120194 |
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